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  Dysregulation of the mesoprefrontal dopamine circuit mediates an early-life stress-induced synaptic imbalance in the prefrontal cortex

Oh, W. C., Rodríguez, G., Asede, D., Jung, K., Hwang, I.-W., Ogelman, R., et al. (2021). Dysregulation of the mesoprefrontal dopamine circuit mediates an early-life stress-induced synaptic imbalance in the prefrontal cortex. Cell Reports, (5). Retrieved from https://www.cell.com/article/S2211124721004058/pdf.

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Genre: Journal Article
Alternative Title : Cell Reports

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 Creators:
Oh, Won Chan1, Author
Rodríguez, Gabriela1, Author
Asede, Douglas1, Author
Jung, Kanghoon1, Author
Hwang, In-Wook1, Author
Ogelman, Roberto1, Author
Bolton, McLean M.1, Author
Kwon, Hyung-Bae1, Author
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1external, ou_persistent22              

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Free keywords: Animals, Male, Mice, synaptic plasticity, dopamine, Prefrontal Cortex, two-photon microscopy, Dopamine, early-life stress, excitatory synapse, inhibitory synapse, PFC, VTA
 Abstract: Stress adversely affects an array of cognitive functions. Although stress-related disorders are often addressed in adulthood, far less is known about how early-life stress (ELS) affects the developing brain in early postnatal periods. Here we show that ELS, induced by maternal separation, leads to synaptic alteration of layer 2/3 pyramidal neurons in the prefrontal cortex (PFC) of mice. We find that layer 2/3 neurons show increased excitatory synapse numbers following ELS and that this is accompanied by hyperexcitability of PFC-projecting dopamine (DA) neurons in the ventral tegmental area. Notably, excitatory synaptic change requires local signaling through DA D2 receptors. In vivo pharmacological treatment with a D2 receptor agonist in the PFC of control mice mimics the effects of ELS on synaptic alterations. Our findings reveal a neuromodulatory mechanism underlying ELS-induced PFC dysfunction, and this mechanism may facilitate a more comprehensive understanding of how ELS leads to mental disorders.

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 Dates: 2021
 Publication Status: Issued
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Title: Cell Reports
  Alternative Title : Cell Rep
Source Genre: Journal
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Pages: 109074 Volume / Issue: (5) Sequence Number: - Start / End Page: - Identifier: ISBN: 2211-1247